Myceloom: The Network Architecture of Living Systems

A Digital Archaeological Investigation

Protocol Specification — A Digital Archaeological Investigation

Josie Jefferson & Felix Velasco
Digital Archaeologists, Unearth Heritage Foundry

with Technical Collaboration from:
Claude 4.5 (Opus & Sonnet) & Gemini (2.5 & 3 Pro)
(Synthetic Intelligence Systems)

Date: January 2026
Version: 1.0
Publication Type: Protocol Specification / Working Paper
Series: The Myceloom Protocol (Part 2 of 8)

Keywords: Myceloom, Network Architecture, Biological Networks, Distributed Systems, Self-Healing Infrastructure, Fault Tolerance, Scale-Free Networks, Mycorrhizal Networks, Adaptive Routing, Network Topology


Abstract

Engineers racing to build faster applications often overlook the most fundamental challenge: creating network architectures that remain coherent under stress, adapt to changing conditions, and scale without sacrificing resilience. This protocol specification defines myceloom network architecture applying biological principles—self-healing, adaptive, fault-tolerant—to digital infrastructure design. Drawing from peer-reviewed research in network science, mycology, and distributed systems theory, this specification establishes why biological network principles offer promising foundations for next-generation digital infrastructure. The document examines scale-free and small-world properties, adaptive routing protocols, and distributed consensus mechanisms operating in mycelial networks for hundreds of millions of years, translating these principles into actionable architectural specifications for building infrastructure that grows, adapts, and heals like living systems.


Introduction: The Architecture Beneath Our Feet

Engineers racing to build faster applications often overlook the most fundamental challenge: creating network architectures that remain coherent under stress, adapt to changing conditions, and scale without sacrificing resilience. Traditional network engineering treats infrastructure as static foundation; rigid protocols constrain rather than enable emergent capabilities. The most resilient distributed systems on Earth demonstrate entirely different principles.

Beneath every forest lies the most sophisticated network architecture evolution has produced. Mycelial networks span continents through interconnected fungal threads exhibiting self-healing properties, adaptive routing protocols, and distributed consensus mechanisms operating without failure for hundreds of millions of years.1 These biological networks achieve fault tolerance, resource optimization, and scalable coordination through architectural principles that challenge fundamental assumptions about network design.

Through digital archaeological excavation, Unearth Heritage Foundry has identified "myceloom" as the network architecture paradigm bridging biological and digital infrastructure design.2 Like underground networks forming the backbone of terrestrial ecosystems, myceloom represents technical substrate upon which resilient, adaptive, distributed systems can be built. Peer-reviewed research in network science, mycology, and distributed systems theory illuminates why biological network principles offer promising foundations for next-generation digital infrastructure.

Implications extend beyond metaphor. Researchers increasingly demonstrate that networks implementing biological principles achieve superior scalability, adaptability, and survivability compared to traditional engineered systems.3 The myceloom framework synthesizes these findings into actionable architectural principles for building infrastructure that grows, adapts, and heals like living systems.


Part I: The Topology of Biological Networks

Network Science Meets Mycology

Recent network science research reveals that mycelial networks exhibit topological properties distinguishing them from both random networks and traditional engineered systems. Mark Fricker, Dan Bebber, and Lynne Boddy at Oxford and Cardiff established that fungal mycelia develop network architectures characterized by high clustering coefficients and efficient global connectivity; these properties optimize both local efficiency and network-wide transport.4

These networks demonstrate emergent topological optimization. Unlike engineered networks designed from centralized specifications, mycelial architectures develop through purely local growth decisions that nonetheless produce globally optimal configurations. Bebber and colleagues demonstrated in their seminal 2007 study that fungal networks achieve transport efficiency comparable to engineered systems while simultaneously maintaining robustness against random damage.5 Traditional network designs struggle to achieve this combination.

Architectural implications are profound. Fricker and colleagues documented in their Microbiology Spectrum review that mycelial networks exhibit continuous reconfiguration in response to environmental cues without compromising network integrity.6 Individual network segments self-organize into higher-order structures through purely local interactions. This achieves global optimization without centralized coordination; conventional distributed systems achieve this only through complex consensus protocols.

Scale-Free and Small-World Properties

Albert-László Barabási and Réka Albert transformed understanding of how complex networks achieve both efficiency and resilience.7 Their 1999 Science paper demonstrated that many natural and technological networks exhibit "scale-free" degree distributions where a few highly connected hubs coexist with many sparsely connected nodes following power-law relationships. This architecture provides robustness against random failures while maintaining short path lengths between any two nodes.

Duncan Watts and Steven Strogatz's 1998 Nature paper on "small-world" networks revealed how systems can simultaneously achieve high local clustering (like regular lattices) and short global path lengths (like random graphs).8 Introducing just a few long-range connections into regular networks dramatically reduces average path lengths while preserving local clustering. This explains phenomena from "six degrees of separation" in social networks to neural architecture efficiency.

Mycelial networks, as Fricker and Boddy documented, exhibit both scale-free and small-world properties through their developmental dynamics.9 Networks establish local hyphal connections through tip growth and branching while developing long-range transport cords creating shortcuts across the network. This dual architecture enables efficient resource distribution at local scales while maintaining network-wide coordination—precisely the combination digital infrastructure architects seek.

Research by Aguilar-Trigueros and colleagues in ISME Communications (2022) demonstrated that network topology serves as a functional trait in fungi.10 Different species exhibit measurably different trade-offs between connectivity, construction cost, transport efficiency, and robustness. Biological networks have evolved diverse architectural strategies optimized for different environmental conditions; this finding has direct implications for designing adaptive digital infrastructure.

Graph-Theoretic Analysis of Mycelial Networks

Applying graph theory to mycelial network analysis has revealed quantitative properties informing engineering design. Network architecture can be characterized through metrics including node degree (connections per junction), betweenness centrality (the proportion of shortest paths passing through a node), and clustering coefficient (the density of connections among a node's neighbors).11

Bebber and colleagues' analysis of Phanerochaete velutina networks demonstrated that fungal architectures achieve "biological solutions to transport network design."12 These topologies balance transport capacity against construction cost and resilience against damage. Networks exhibited path lengths comparable to theoretical optima while maintaining redundancy enabling continued function after significant damage.

This work established methodologies now applied across disciplines. Newman documented in his foundational network science review that tools developed for analyzing biological networks have proven applicable to understanding systems from the Internet to social networks to metabolic pathways.13 The myceloom framework draws on this cross-disciplinary foundation to translate biological insights into engineering principles.


Part II: The Protocol Stack of Nature

Multi-Modal Communication Systems

Mycelial networks operate through sophisticated protocol stacks: layered communication systems enabling seamless interaction between disparate network components. Research by Fricker and colleagues revealed that fungal networks implement multiple transport systems including electrical signaling, chemical communication, and hydraulic resource distribution operating simultaneously across different temporal and spatial scales.14

This multilayered approach challenges traditional network design assumptions. Rather than implementing single-purpose protocols, mycelial networks demonstrate protocol multiplexing—simultaneous operation of multiple communication channels enhancing rather than interfering with each other. Individual network segments participate in electrical signaling for rapid coordination, chemical messaging for resource requests, and hydraulic transport for material distribution, all through the same physical infrastructure.

Transport velocity in mycelial systems demonstrates the efficiency of these biological protocols. Fricker and colleagues documented water transport velocities of 27-148 cm/hour in cord-forming fungi, with solute transport ranging from 10-100 mm/hour depending on cord development.15 These transport rates, achieved through purely biological mechanisms, approach or exceed rates in engineered microfluidic systems while operating without external energy inputs beyond the organism's metabolic processes.

Stigmergic Coordination

Coordination mechanisms in biological networks offer insights directly applicable to distributed system design. Stigmergy—indirect coordination through environmental modification—was first described by Pierre-Paul Grassé in 1959 studying termite nest construction and has since been recognized as a fundamental principle in distributed biological systems.16

Marco Dorigo's development of Ant Colony Optimization algorithms in the 1990s demonstrated that stigmergic principles could be translated into practical computational methods.17 His work, initially published as a doctoral thesis and subsequently in IEEE journals, showed that artificial systems implementing pheromone-trail-like mechanisms could solve complex optimization problems including routing, scheduling, and resource allocation.18

The ACO approach has proven particularly effective for network routing. Di Caro and Dorigo's AntNet algorithm demonstrated that stigmergic routing achieves adaptive, fault-tolerant path selection in telecommunications networks.19 The algorithm maintains routing tables through distributed agents depositing virtual pheromone on successful paths; this creates emergent optimization without centralized control. Contemporary research continues extending these principles, with applications ranging from mobile ad-hoc networks to Internet of Things systems.20

Swarm Intelligence and Distributed Computation

The broader field of swarm intelligence, as synthesized by Bonabeau, Dorigo, and Theraulaz, provides theoretical foundations for understanding how simple agents following local rules can generate globally optimal behaviors.21 Their framework identifies key principles: positive feedback (amplification of successful strategies), negative feedback (preventing premature convergence), randomness (enabling exploration), and multiple interactions (enabling information sharing).

These principles map directly onto observed mycelial network behaviors. Fungal networks exhibit positive feedback through resource allocation to successful transport routes, negative feedback through regression of unsuccessful pathways, exploration through tip growth into new territories, and information integration through network-wide transport dynamics.22 The myceloom framework recognizes these correspondences as more than analogy; they represent convergent solutions to fundamental challenges in distributed coordination.


Part III: The Resilience Architecture

Fault Tolerance Through Redundancy

Mycelial networks demonstrate the most sophisticated fault tolerance mechanisms documented in distributed systems. Research by Fricker and colleagues revealed that these biological networks can lose substantial portions of their physical structure while maintaining network connectivity and transport function.23 Networks achieve this resilience through architectural principles treating failure as a normal operating condition rather than an exceptional circumstance.

The biological approach to network resilience operates through redundant pathway development, adaptive rerouting, and continuous network reconstruction. Rather than implementing expensive failover mechanisms, mycelial networks continuously grow new connections, reinforce successful pathways, and allow unsuccessful routes to degrade naturally. This creates networks that become stronger under stress rather than weaker; they exhibit what Nassim Taleb terms "antifragility."24

In-silico analysis of fungal network robustness by Fricker's group demonstrated species-specific resilience strategies.25 Phanerochaete velutina networks showed different failure modes than Phallus impudicus; the former breaking down more rapidly under random attack but exhibiting greater efficiency under normal conditions. This trade-off between efficiency and robustness parallels engineering decisions in digital network design.

Byzantine Fault Tolerance and Consensus

Maintaining system coherence despite component failures has occupied distributed systems researchers since Lamport, Shostak, and Pease's foundational work on the "Byzantine Generals Problem."26 Their 1982 paper established that distributed systems can reach consensus despite arbitrary (Byzantine) failures provided fewer than one-third of components are faulty. This result has profound implications for fault-tolerant system design.

Subsequent work, particularly Castro and Liskov's Practical Byzantine Fault Tolerance (PBFT) algorithm, demonstrated that Byzantine consensus could be achieved with acceptable overhead in real systems.27 PBFT and its descendants now underpin blockchain systems, distributed databases, and critical infrastructure requiring consensus among potentially unreliable participants.

The myceloom framework recognizes parallels between biological and computational fault tolerance. Mycelial networks achieve consensus-like behaviors—coordinated resource allocation, synchronized growth responses, collective defense against pathogens—through mechanisms tolerating component failure without centralized coordination.28 While specific mechanisms differ from PBFT, functional outcomes suggest convergent solutions to reliable coordination among unreliable components.

Self-Stabilization and Healing

Dijkstra's foundational 1974 paper on self-stabilizing systems established principles for distributed systems automatically recovering from transient faults.29 Self-stabilizing systems guarantee convergence to correct behavior from any initial state, providing resilience against memory corruption, message loss, and other transient failures.

Mycelial networks exhibit biological self-stabilization through continuous growth, regression, and reconstruction dynamics. Damaged portions trigger compensatory growth in adjacent regions; failed transport routes are replaced by alternative pathways; resources are reallocated from unsuccessful to successful network segments.30 These dynamics ensure network recovery without explicit failure detection or repair protocols.

Contemporary research increasingly combines Byzantine fault tolerance with self-stabilization to create systems resilient to both permanent and transient failures.31 The myceloom framework draws on both traditions, recognizing that sustainable infrastructure must handle the full spectrum of failure modes biological systems have evolved to address.


Part IV: The Infrastructure of Symbiosis

Collaborative Network Architecture

The myceloom architectural framework recognizes that sustainable network infrastructure must enable rather than constrain collaborative relationships between diverse system components. Drawing from mycorrhizal network research, myceloom architectures prioritize interoperability, resource sharing, and mutual enhancement over traditional metrics like throughput optimization or latency minimization.32

This represents a shift in network design philosophy. Rather than treating the network as passive transport medium, myceloom architectures operate as active collaboration platforms enhancing connected system capabilities. Research in mycorrhizal ecology demonstrates that networks implementing symbiotic principles achieve emergent capabilities exceeding the sum of individual component capacities; "network effects" in a literal sense.33

Suzanne Simard's research on "mother trees" and forest communication networks revealed that mycorrhizal connections enable resource transfer between plants, with older trees supporting seedlings and stressed neighbors through the underground network.34 While subsequent research has debated the extent and mechanisms of such transfers, the principle that network architecture enables rather than constrains collaboration remains foundational to the myceloom framework.

Commons Governance and Protocol Design

Designing collaborative network infrastructure intersects with research on commons governance pioneered by Elinor Ostrom.35 Her analysis of successful common-pool resource systems identified design principles: clear boundaries, proportional costs and benefits, collective choice arrangements, monitoring, graduated sanctions, conflict resolution mechanisms, and recognition by higher authorities.

These principles translate into protocol design considerations for myceloom networks. Effective collaborative infrastructure requires mechanisms for defining participation boundaries, ensuring fair resource allocation, enabling collective decision-making about network evolution, detecting and responding to protocol violations, and interfacing with external governance systems.36 The myceloom framework incorporates these considerations into its architectural principles.


Part V: Distributed Intelligence Infrastructure

Emergence Without Centralization

Mycelial networks demonstrate that sophisticated coordination can emerge from distributed intelligence rather than centralized control systems. Research reveals that fungal networks exhibit collective decision-making capabilities emerging from local interactions between network components without requiring global coordination mechanisms.37

This biological insight transforms thinking about network management and coordination. Rather than implementing centralized network management systems, myceloom architectures enable distributed coordination where network intelligence emerges from interactions between autonomous network segments. Individual components make local decisions based on immediate conditions while contributing to network-wide optimization patterns.

Theoretical foundations for understanding such emergence draw on complex adaptive systems research by scholars including Stuart Kauffman, John Holland, and Melanie Mitchell.38 Their work established that systems composed of many interacting components can exhibit emergent behaviors not predictable from component properties alone; this phenomenon is central to understanding both biological and computational networks.

Network Learning and Adaptation

Recent research has explored whether mycelial networks exhibit learning-like capabilities. Adamatzky's work on slime mold computing demonstrated that Physarum polycephalum can solve computational problems including shortest path finding and network optimization.39 While mechanisms differ from neural computation, these findings suggest biological networks can implement forms of distributed intelligence.

Implications extend to network governance and evolution. Myceloom networks can adapt their own architectures in response to changing requirements without requiring manual reconfiguration or centralized planning. Research suggests that self-evolving networks represent the future of distributed systems architecture; infrastructure that learns from its operation and automatically optimizes its configuration.40


Part VI: The Future of Living Infrastructure

Toward Bio-Hybrid Systems

Emerging research documents that technological infrastructure is evolving toward architectures incorporating biological principles at fundamental levels.41 The convergence of synthetic biology, materials science, and computer engineering enables systems blurring the boundary between living and technological systems.

Research on unconventional computing explores how biological substrates might directly implement computational functions. Adamatzky's investigations of fungal computing demonstrated that mycelial networks exhibit electrical signaling properties potentially applicable to information processing.42 While practical fungal computers remain speculative, the research illuminates how biological architectures might inform computational design at fundamental levels.

The myceloom framework anticipates this convergence, providing architectural principles applicable to both purely digital systems and emerging bio-hybrid technologies. Whether implemented in silicon or mycelium, principles of adaptive topology, distributed coordination, and resilient redundancy remain applicable.

Energy Efficiency and Sustainability

Contemporary research increasingly emphasizes the energy efficiency of biological computation compared to conventional electronic systems.43 Mycelial networks operate on solar energy captured by photosynthetic partners, achieving computational and coordination functions without the energy demands of data centers and network infrastructure.

This efficiency stems from architectural principles rather than mere substrate differences. Biological networks achieve function through adaptive structure rather than brute-force computation; they implement "computation" through physical reconfiguration rather than abstract symbol manipulation.44 The myceloom framework draws on these insights to inform energy-efficient digital infrastructure design.


Part VII: Implementation Principles

The Network of Networks

The myceloom framework culminates in practical network architecture: protocols, topologies, and coordination mechanisms enabling construction of "networks of networks" operating like biological ecosystems.45 Unlike traditional internet architecture treating networks as isolated systems occasionally connected through rigid protocols, myceloom architectures enable seamless integration and collaborative enhancement between diverse network systems.

This represents fundamental evolution in distributed systems design. Rather than building networks constraining interaction within predetermined protocols, myceloom frameworks provide adaptive infrastructure enabling systems to develop novel collaboration forms based on emerging needs and opportunities.

Practical applications are transformative. Network architects can implement myceloom principles through modular architectures enabling network segments to adapt, evolve, and collaborate based on usage patterns rather than predetermined specifications. These approaches demonstrate how biological principles can inform network infrastructure honoring both technical efficiency and collaborative potential.

Design Principles for Myceloom Networks

Drawing on surveyed research, the myceloom framework identifies key architectural principles:

Adaptive Topology: Networks should continuously reconfigure based on usage patterns and environmental conditions, like mycelial networks growing toward resources and regressing from unproductive areas.46

Distributed Coordination: Global optimization should emerge from local decisions without centralized control, implementing stigmergic or consensus-based coordination appropriate to the application domain.47

Redundant Pathways: Critical functions should be supported by multiple independent pathways, enabling graceful degradation rather than catastrophic failure under stress.48

Protocol Multiplexing: Networks should support multiple simultaneous communication modalities, enabling different types of interaction through the same infrastructure.49

Collaborative Enhancement: Network architecture should enable connected systems to enhance each other's capabilities rather than merely coexist.50

Self-Stabilization: Networks should automatically recover from transient failures and adapt to permanent changes without manual intervention.51

These principles, grounded in peer-reviewed research on biological and computational networks, provide foundations for designing infrastructure that grows, adapts, and heals like living systems.


Conclusion: The Living Network Substrate

The linguistic innovation of "myceloom" provides essential terminology for network architecture transcending traditional infrastructure limitations. Rather than describing "adaptive distributed network protocols with biological coordination mechanisms," one speaks of myceloom architectures and immediately conveys essential qualities: organic, resilient, collaborative, intelligent.

As distributed systems advance, the mycelial networks beneath the forest floor offer profound lessons about network topology, protocol design, and distributed coordination. The future of network architecture may lie not in perfecting isolated systems, but in weaving them into living infrastructures demonstrating nature's most effective approaches to distributed intelligence.

The myceloom framework captures this evolution: network architectures growing like biological systems, adapting like living organisms, demonstrating the collaborative resilience necessary for supporting complex distributed applications.52 In this convergence of biological wisdom and network engineering lies not just technical innovation, but pathways toward infrastructure enhancing rather than constraining the collaborative potential of connected systems.

The backbone metaphor becomes literal: myceloom networks provide living infrastructure through which distributed systems achieve the resilience, adaptability, and collaborative intelligence biological networks have demonstrated for hundreds of millions of years.


Notes


Bibliography

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Adamatzky, Andrew, ed. Advances in Unconventional Computing. 2 vols. Cham: Springer, 2017.

Aguilar-Trigueros, Carlos A., Lynne Boddy, Matthias C. Rillig, and Mark D. Fricker. "Network Traits Predict Ecological Strategies in Fungi." ISME Communications 2, no. 2 (2022): 1-11.

Albert, Réka, and Albert-László Barabási. "Statistical Mechanics of Complex Networks." Reviews of Modern Physics 74, no. 1 (2002): 47-97.

Barabási, Albert-László, and Réka Albert. "Emergence of Scaling in Random Networks." Science 286, no. 5439 (1999): 509-512.

Bebber, Daniel P., Juliet Hynes, Peter R. Darrah, Lynne Boddy, and Mark D. Fricker. "Biological Solutions to Transport Network Design." Proceedings of the Royal Society B: Biological Sciences 274, no. 1623 (2007): 2307-2315.

Blum, Christian. "Ant Colony Optimization: Introduction and Recent Trends." Physics of Life Reviews 2, no. 4 (2005): 353-373.

Bonabeau, Eric, Marco Dorigo, and Guy Theraulaz. Swarm Intelligence: From Natural to Artificial Systems. New York: Oxford University Press, 1999.

Castro, Miguel, and Barbara Liskov. "Practical Byzantine Fault Tolerance." In Proceedings of the Third Symposium on Operating Systems Design and Implementation, 173-186. New Orleans: USENIX Association, 1999.

Di Caro, Gianni, and Marco Dorigo. "AntNet: Distributed Stigmergetic Control for Communications Networks." Journal of Artificial Intelligence Research 9 (1998): 317-365.

Dijkstra, Edsger W. "Self-Stabilizing Systems in Spite of Distributed Control." Communications of the ACM 17, no. 11 (1974): 643-644.

Dolev, Shlomi. Self-Stabilization. Cambridge, MA: MIT Press, 2000.

Dorigo, Marco. "Optimization, Learning and Natural Algorithms." PhD diss., Politecnico di Milano, 1992.

Dorigo, Marco, and Christian Blum. "Ant Colony Optimization Theory: A Survey." Theoretical Computer Science 344, no. 2-3 (2005): 243-278.

Dorigo, Marco, Vittorio Maniezzo, and Alberto Colorni. "Ant System: Optimization by a Colony of Cooperating Agents." IEEE Transactions on Systems, Man, and Cybernetics, Part B 26, no. 1 (1996): 29-41.

Fricker, Mark D., Dan Bebber, and Lynne Boddy. "Mycelial Networks: Structure and Dynamics." In Ecology of Saprotrophic Basidiomycetes, edited by Lynne Boddy, Juliet C. Frankland, and Pieter van West, 3-18. London: Academic Press, 2008.

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Fricker, Mark D., Luke L. M. Heaton, Nick S. Jones, and Lynne Boddy. "The Mycelium as a Network." Microbiology Spectrum 5, no. 3 (2017): FUNK-0033-2017.

Fricker, Mark D., Juliet A. Lee, Dan P. Bebber, Monika Tlalka, Juliet Hynes, Peter R. Darrah, Sarah C. Watkinson, and Lynne Boddy. "Imaging Complex Nutrient Dynamics in Mycelial Networks." Journal of Microscopy 231, no. 2 (2008): 317-331.

Grassé, Pierre-Paul. "La Reconstruction du Nid et les Coordinations Interindividuelles chez Bellicositermes Natalensis et Cubitermes sp." Insectes Sociaux 6, no. 1 (1959): 41-80.

Gross, Thilo, and Hiroki Sayama, eds. Adaptive Networks: Theory, Models and Applications. Berlin: Springer, 2009.

Lamport, Leslie, Robert Shostak, and Marshall Pease. "The Byzantine Generals Problem." ACM Transactions on Programming Languages and Systems 4, no. 3 (1982): 382-401.

Mitchell, Melanie. Complexity: A Guided Tour. New York: Oxford University Press, 2009.

Newman, Mark E. J. "The Structure and Function of Complex Networks." SIAM Review 45, no. 2 (2003): 167-256.

Ostrom, Elinor. "Beyond Markets and States: Polycentric Governance of Complex Economic Systems." American Economic Review 100, no. 3 (2010): 641-672.

Ostrom, Elinor. Governing the Commons: The Evolution of Institutions for Collective Action. Cambridge: Cambridge University Press, 1990.

Simard, Suzanne W. "Mycorrhizal Networks: A Review of Their Extent, Function, and Importance." Canadian Journal of Botany 90, no. 4 (2012): 277-321.

Simard, Suzanne W., et al. "Net Transfer of Carbon Between Ectomycorrhizal Tree Species in the Field." Nature 388, no. 6642 (1997): 579-582.

Strubell, Emma, Ananya Ganesh, and Andrew McCallum. "Energy and Policy Considerations for Deep Learning in NLP." In Proceedings of the 57th Annual Meeting of the Association for Computational Linguistics, 3645-3650. Florence: Association for Computational Linguistics, 2019.

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Webster-Wood, Victoria A., et al. "Biohybrid Robots: Recent Progress, Challenges, and Perspectives." Bioinspiration & Biomimetics 18, no. 1 (2023): 015001.


1 Mark D. Fricker, Luke L. M. Heaton, Nick S. Jones, and Lynne Boddy, "The Mycelium as a Network," Microbiology Spectrum 5, no. 3 (2017): FUNK-0033-2017, https://doi.org/10.1128/microbiolspec.FUNK-0033-2017.
2 Unearth Heritage Foundry, "Myceloom," in The Unearth Lexicon of Digital Archaeology (2025), https://unearth.wiki. See also Vivibyte, Network Architecture, Distributed Systems.
3 Christian Blum, "Ant Colony Optimization: Introduction and Recent Trends," Physics of Life Reviews 2, no. 4 (2005): 353-373.
4 Mark D. Fricker, Dan Bebber, and Lynne Boddy, "Network Organisation of Mycelial Fungi," in Biology of the Fungal Cell, ed. R. J. Howard and N. A. R. Gow (Berlin: Springer, 2007), 309-330.
5 Daniel P. Bebber, Juliet Hynes, Peter R. Darrah, Lynne Boddy, and Mark D. Fricker, "Biological Solutions to Transport Network Design," Proceedings of the Royal Society B: Biological Sciences 274, no. 1623 (2007): 2307-2315.
6 Fricker et al., "The Mycelium as a Network."
7 Albert-László Barabási and Réka Albert, "Emergence of Scaling in Random Networks," Science 286, no. 5439 (1999): 509-512.
8 Duncan J. Watts and Steven H. Strogatz, "Collective Dynamics of 'Small-World' Networks," Nature 393, no. 6684 (1998): 440-442.
9 Mark D. Fricker, Dan Bebber, and Lynne Boddy, "Mycelial Networks: Structure and Dynamics," in Ecology of Saprotrophic Basidiomycetes, ed. Lynne Boddy, Juliet C. Frankland, and Pieter van West (London: Academic Press, 2008), 3-18.
10 Carlos A. Aguilar-Trigueros, Lynne Boddy, Matthias C. Rillig, and Mark D. Fricker, "Network Traits Predict Ecological Strategies in Fungi," ISME Communications 2, no. 2 (2022): 1-11.
11 Réka Albert and Albert-László Barabási, "Statistical Mechanics of Complex Networks," Reviews of Modern Physics 74, no. 1 (2002): 47-97.
12 Bebber et al., "Biological Solutions to Transport Network Design."
13 Mark E. J. Newman, "The Structure and Function of Complex Networks," SIAM Review 45, no. 2 (2003): 167-256.
14 Mark D. Fricker, Juliet A. Lee, Dan P. Bebber, Monika Tlalka, Juliet Hynes, Peter R. Darrah, Sarah C. Watkinson, and Lynne Boddy, "Imaging Complex Nutrient Dynamics in Mycelial Networks," Journal of Microscopy 231, no. 2 (2008): 317-331.
15 Fricker et al., "The Mycelium as a Network."
16 Pierre-Paul Grassé, "La Reconstruction du Nid et les Coordinations Interindividuelles chez Bellicositermes Natalensis et Cubitermes sp. La Théorie de la Stigmergie: Essai d'Interprétation du Comportement des Termites Constructeurs," Insectes Sociaux 6, no. 1 (1959): 41-80.
17 Marco Dorigo, "Optimization, Learning and Natural Algorithms" (PhD diss., Politecnico di Milano, 1992).
18 Marco Dorigo, Vittorio Maniezzo, and Alberto Colorni, "Ant System: Optimization by a Colony of Cooperating Agents," IEEE Transactions on Systems, Man, and Cybernetics, Part B 26, no. 1 (1996): 29-41.
19 Gianni Di Caro and Marco Dorigo, "AntNet: Distributed Stigmergetic Control for Communications Networks," Journal of Artificial Intelligence Research 9 (1998): 317-365.
20 Marco Dorigo and Christian Blum, "Ant Colony Optimization Theory: A Survey," Theoretical Computer Science 344, no. 2-3 (2005): 243-278.
21 Eric Bonabeau, Marco Dorigo, and Guy Theraulaz, Swarm Intelligence: From Natural to Artificial Systems (New York: Oxford University Press, 1999).
22 Fricker et al., "Mycelial Networks: Structure and Dynamics."
23 Bebber et al., "Biological Solutions to Transport Network Design."
24 Nassim Nicholas Taleb, Antifragile: Things That Gain from Disorder (New York: Random House, 2012).
25 Fricker et al., "The Mycelium as a Network."
26 Leslie Lamport, Robert Shostak, and Marshall Pease, "The Byzantine Generals Problem," ACM Transactions on Programming Languages and Systems 4, no. 3 (1982): 382-401.
27 Miguel Castro and Barbara Liskov, "Practical Byzantine Fault Tolerance," in Proceedings of the Third Symposium on Operating Systems Design and Implementation (New Orleans: USENIX Association, 1999), 173-186.
28 Fricker et al., "The Mycelium as a Network."
29 Edsger W. Dijkstra, "Self-Stabilizing Systems in Spite of Distributed Control," Communications of the ACM 17, no. 11 (1974): 643-644.
30 Fricker et al., "Mycelial Networks: Structure and Dynamics."
31 Shlomi Dolev, Self-Stabilization (Cambridge, MA: MIT Press, 2000).
32 Suzanne W. Simard, "Mycorrhizal Networks and Seedling Establishment in Douglas-Fir Forests," in Ecology and Management of Pinyon-Juniper Communities (Ogden, UT: USDA Forest Service, 1999), 260-263.
33 Suzanne W. Simard et al., "Net Transfer of Carbon Between Ectomycorrhizal Tree Species in the Field," Nature 388, no. 6642 (1997): 579-582.
34 Suzanne W. Simard, "Mycorrhizal Networks: A Review of Their Extent, Function, and Importance," Canadian Journal of Botany 90, no. 4 (2012): 277-321.
35 Elinor Ostrom, Governing the Commons: The Evolution of Institutions for Collective Action (Cambridge: Cambridge University Press, 1990).
36 Elinor Ostrom, "Beyond Markets and States: Polycentric Governance of Complex Economic Systems," American Economic Review 100, no. 3 (2010): 641-672.
37 Fricker et al., "The Mycelium as a Network."
38 Melanie Mitchell, Complexity: A Guided Tour (New York: Oxford University Press, 2009).
39 Andrew Adamatzky, ed., Advances in Unconventional Computing, 2 vols. (Cham: Springer, 2017).
40 Thilo Gross and Hiroki Sayama, eds., Adaptive Networks: Theory, Models and Applications (Berlin: Springer, 2009).
41 Victoria A. Webster-Wood et al., "Biohybrid Robots: Recent Progress, Challenges, and Perspectives," Bioinspiration & Biomimetics 18, no. 1 (2023): 015001.
42 Andrew Adamatzky, "Towards Fungal Computer," Interface Focus 8, no. 6 (2018): 20180029.
43 Emma Strubell, Ananya Ganesh, and Andrew McCallum, "Energy and Policy Considerations for Deep Learning in NLP," in Proceedings of the 57th Annual Meeting of the Association for Computational Linguistics (Florence: Association for Computational Linguistics, 2019), 3645-3650.
44 Adamatzky, Advances in Unconventional Computing.
45 Unearth Heritage Foundry, "Myceloom," in The Unearth Lexicon of Digital Archaeology (2025), https://unearth.wiki.
46 Fricker et al., "Mycelial Networks: Structure and Dynamics."
47 Dorigo and Blum, "Ant Colony Optimization Theory."
48 Bebber et al., "Biological Solutions to Transport Network Design."
49 Fricker et al., "Imaging Complex Nutrient Dynamics in Mycelial Networks."
50 Simard, "Mycorrhizal Networks."
51 Dijkstra, "Self-Stabilizing Systems in Spite of Distributed Control."
52 Unearth Heritage Foundry, "Myceloom," in The Unearth Lexicon of Digital Archaeology (2025), https://unearth.wiki.